Insecticide Thiamethoxam: A Bioactive Action on Carrot Seeds Daucus carota L.. Root length cm of seedlings of four seed lots of carrot, cultivar Brasilia, without A and with B water stre
Trang 1Insecticide Thiamethoxam: A Bioactive Action on Carrot Seeds (Daucus carota L.) 9
balance of the plant, tolerating water deficit better (Castro, 2006) As observed in soybean root development increases the absorption of nutrients, increases the expression of leaf area and plant vigor (Tavares and Castro, 2005)
The data speed of germination, without (Figure 5A) and with (Figure 5B) stress show that the treated seeds had a higher rate compared to control The concentrations used had similar results Treated seeds germinated on average one day soon if they have not been subjected
to water stress and two days are subject to stress This effect is very promising because carrot seeds in field conditions have poor germination, slow and irregular resulting in uneven emergence (Corbineau et al., 1994) This increased speed of germination is caused by physiological changes that occur in the plant indirectly stimulating the production of hormones, resulting in increased vigor, root growth, water absorption and primary and secondary metabolism, as observed in the sugarcane crop (Castro, 2007)
*
*
*
1 3 5 7 9 11 13
Lotes
0,05mL/l 0,0mL/l
(A)
*
0 2 4 6 8 10
Lotes
0,4mL/l 0,05mL/l 0,0mL/l
(B) Fig 3 Root length (cm) of seedlings of four seed lots of carrot, cultivar Brasilia, without (A) and with (B) water stress * Different from the control by Dunnet test at probability level
of 5%
Lots
Lots
Trang 2(A)
mL of product/ 3g of seed
Fig 4 Root length (cm) of seedlings of four seed lots of carrot, cultivar Brasilia, without (A) and with (B) water stress
Trang 3Insecticide Thiamethoxam: A Bioactive Action on Carrot Seeds (Daucus carota L.) 11
*
*
*
*
0
1
2
3
4
5
6
Lotes
0,4mL/l 0,05mL/l 0,0mL/l
(A)
0 1 2 3 4 5 6 7
Lotes
0,4mL/l 0,05mL/l 0,0mL/l
(B)
Fig 5 Speed of germination (days) of four seed lots of carrot cultivar Brasilia, without (A) and with (B) water stress.* It differs from the control by Dunnet test at probability level of 5%
Trang 4* * * * * * * *
40 50 60 70 80 90 100
Lotes
0,4mL/l 0,05mL/l 0,0mL/l
(A)
40 50 60 70 80 90 100
Lotes
0,4mL/l 0,05mL/l 0,0mL/l
Fig 6 Emergence of seedlings in the greenhouse for four seed lots of carrot, cultivar Brasilia without (A) and with (B) water stress * Different from the control by Dunnet test at
probability level of 5%
Lots
Lots
Trang 5Insecticide Thiamethoxam: A Bioactive Action on Carrot Seeds (Daucus carota L.) 13
In Figure 6, without (Figure 6A) and with (Figure 6B) water stress, it was observed that the emergence of seedlings in the greenhouse was stimulated, and the seeds treated with thiamethoxam showed significant differences compared to control The positive differences compared to control vary according to lots, 9 to 17 percentage points if the seeds have not been subjected to water stress and 20 to 10 percentage points when subjected to stress The two concentrations showed similar responses These results confirm those found in soybean, to be seen increase in the root system and the percentage
of seedling emergence also in water deficit conditions (Castro et al., 2006) According to the literature, soybean seeds treated with thiamethoxam have higher levels of amino acids, enzyme activity and synthesis of plant hormones that increase the plant responses
to these proteins and these events provide significant increases in production and reducing the time of establishment of culture in the field, making it more tolerant to stress factors (Castro, 2006)
The results obtained can be described that the product stimulated the performance of carrot seeds in all parameters evaluated, both in seeds subjected to water stress or not Carrot seeds treated with the product thiamethoxam showed significant increases in germination and vigor for all lots Among the aspects of vigor, the product stimulated the growth of the root length, which is of great importance to the culture of carrots and this result was obtained in the laboratory confirmed in the greenhouse
The product was more effective in stimulating the quality of seeds not subjected to water stress, with the exception of root length which positive change was similar for seeds subjected to stress or not In all parameters evaluated, increases in the quality varied according to the lot Concentrations of the product for most tests evaluated did not differ, however there was a trend of higher concentration to the higher values
The application of thiamethoxam has strong interest for the culture of carrot, whose edible portion is the root and, moreover, by presenting, in field conditions, poor germination, slow, irregular with uneven emergence, the product acts as an enhancer, by allowing the expression of seed germination potential, accelerate the growth of roots and increase the absorption of nutrients by the plant These features of thiamethoxam combined with the use
of genetics and physiological high-quality seed powers the productive capacity of the culture
5 Conclusions
Thiamethoxam product stimulates the physiological performance of carrot seeds subjected
to water stress or not, with variable intensity according to lot
Concentrations of 0.05 and 0.4 mL of the product is effective, however there is a tendency of higher concentration to the higher increases in quality
6 References
ALMEIDA, A.S.; TILLMANN, M.A.A.; VILLELA, F A.; PINHO, M.S Bioativador no
desempenho fisiológico de sementes de cenoura Revista Brasileira de Sementes, Brasília,v.31, n 3, p 87-95, 2009
Trang 6ANANIA, F.R.; TEIXEIRA, N.T.; CALAFIORI, M.H.; ZAMBON,S Influência de inseticidas
granulados sistêmicos nos teores de N-P-K nas folhas de amendoim (Arachis hypogaea L.) Ecossistema, Espírito Santo do Pinhal, v 13, p 121-124, 1988a
ANANIA, P,F.R.; TEIXEIRA, N.T.; CALAFIORI, M.H.; ZAMBON,S Influência de inseticidas
granulados sistêmicos nos teores de N-P-K nas folhas de limoeiro Taiti (Citrus aurantifolia.) cv Peruano Ecossistema, Espírito Santo do Pinhal, v 13, p 121-124,
1988b
CALAFIORI, M.H; TEIXEIRA, N.T; SCHMIDT, H A P.; ANANIA, P.F.R.; GRANDO, F.I.;
PALAZZINI, R.; MARTINS, R.C.; OLIVEIRA, C.L.; ZAMBON, S Efeitos nutricionais de inseticidas sistêmicos granulados sobre cafeeiros Ecossistema Espírito Santo do Pinhal, v.14.p 132-14, 1989
CASTRO, P.R.C.; PITELLI, A M.C.M.; PERES, L.E.P.; ARAMAKI, P.H Análise da atividade
hormonal de thiametoxam através de biotestes Publicatio, UEPG, 2007
CASTRO, P.R.C Agroquimicos de controle hormonal na agricultura tropical Boletim, n.32,
Série Produtor Rural, USP/ ESALQ/ DIBD, Piracicaba, 46p., 2006
CASTRO, P.R.C.; PITELLI, AM.C.M.; PERES, L.E.P Avaliação do crescimento da raiz e parte
aérea de plântulas de tomateiro MT, DGT E BRT germinadas em diferentes concentrações do inseticida thiametoxan In ESCOLA SUPERIOR DE AGRICULTURA “LUIZ DE QUEIROZ” Relatório técnico ESALQ/Syngenta Piracicaba, p.14-25, 2005
CASTRO, P.R.C.; SOARES, F.C.; ZAMBON, S.; MARTINS, A N.; Efeito do aldicarb no
desenvolvimento do feijoeiro cultivar Carioca Ecossistema Espírito Santo do Pinhal, v.20, p 63-68, 1995
CATANEO, A C.; ANDRÉO, Y.; SEIFFERT, M.; BÚFALO,J.; FERREIRA,L.C Ação do
inseticida Cruiser sobre a germinação do soja em condições de estresse In: IVCONGRESSO BRASILEIRO DE SOJA, Resumos, Londrina, p.90,
2006
CORBINEAU, F.; PICARDE, M.A.; CÔME, D Effects of temperature, oxigen and osmotic
pressure on germination of carrot seeds: evaluation of seed quality Acta Horticulturae, The Hague, v.354, p.9-15, 1994
De GRANDE, P.E Influência de aldicarb e carbofuran na soja (Glycine max L.) Merrill 137f
Dissertação (Mestrado em Entomologia) - Escola Superior de Agricultura “Luiz de Queiroz”, Universidade de São Paulo, Piracicaba, 1992
DENARDIN, N.D Ação do thiametoxan sobre a fixação biológica do nitrogênio e na
promoção de ativadores de crescimento vegetal In: Universidade de Passo Fundo Relatório técnico, Passo Fundo, 2005
HORII, A; McCUE, P.; SHETTY, K Enhancement of seed vigour following and phenolic
elicitor treatment Bioresource Technology, United States, v.98, n.3, p.623-632,
2007
JUNQUEIRA, F.M.A; FORNER, M.A; CALAFIORI, M.H.; TEIXEIRA, N.T.; ZAMBON, S.;
Aplicação de aldicarb em diferentes dosagens e tipos de adubação influenciando a
produtividade na cultura da batata (Solarium tuberosum L.) Ecossistema, Espírito
Santo do Pinhal, v 13, p 101-107, 1988
Trang 7Insecticide Thiamethoxam: A Bioactive Action on Carrot Seeds (Daucus carota L.) 15
LAUXEN, L.R.; VILLELA, F A.; SOARES, R C Desempenho fisiológico de sementes de
algodão tratadas com tiametoxam Revista Brasileira de Sementes Brasília, v 32, n
3, p 61-68 , 2010
LUBUS, C.A.F.; FERRAZ, J.A.D.P.; CALAFIORI, M.H.; ZAMBON, S.; BUENO, B.F Ensaio
com diferentes dosagens de aldicard e de adubo visando a produtividade na
cultura da batata (Solarium tuberosum L.), Ecossistema, Espírito Santo do Pinhal, v
10, p 64-66, 1985
MAGUIRE, J.D Speed of germination and in selection and evaluation for
seedling emergence and vigor Crop Science, Madison, v.2, n.2, p.176-177,
1962
NUNES, J.C Bioativador de plantas: uma utilidade adicional para um produto
desenvolvido originalmente como inseticida Revista SEEDNews, Pelotas, v.10, n.5, p.30-31, 2006
OLIVEIRA, V.S.; LIMA, J.M.; CARVALHO, R.F.; RIGITANO, R.L.O Absorção do inseticida
tiametoxam em latossolos sob efeito de fosfato e vinhaça Revista Química Nova, Lavras, v 32, n 6, p 1432-1435, 2009
PEREIRA, M.A.; CASTRO, P.R.C.; GARCIA, E.O; REIS, A R Efeitos fisiológicos de
Thiametoxan em plantas de feijoeiro In: XI CONGRESSO BRASILEIRO DE FISIOLOGIA VEGETAL, Resumos, Gramado: Sociedade Brasileira de Fisiologia Vegetal, 2007
REDDY, K.R.; REDDY, V.R.; BAKER, D.N.; McKINION, J.M Effects of aldicarb on
photosynthesis, root growth and flowering of cotton In: PLANT GROWTH REGULATION SOCIETY OF AMERICAN ANNUAL MEETING, 16., Arlington Proceedings… Arligton: Plant Regulation Society of American, p.168-169,
1989
REDDY, K.R.; REDDY, V.R.; BAKER, D.N.; McKINION, J.M Is aldicarb a plant growth
regulator In PLANT GROWTH REGULATION SOCIETY OF AMERICAN ANNUAL MEETING, 17., Proceedings… Saint Paul: Plant Regulation Society of American, p.79-80, 1990
TAVARES, S.; CASTRO, P.R.C.; RIBEIRO, R.V.; ARAMAKI, P.H Avaliação dos efeitos
fisiológicos do tiametoxam no tratamento de sementes de soja Revista da Agricultura, Piracicaba, 2007
TAVARES, S.; CASTRO, P.R.C Avaliação dos efeitos fisiológicos de Cruiser 35FS após
tratamento de sementes de soja In: ESCOLA SUPERIOR DE AGRICULTURA
“LUIZ DE QUEIROZ” Relatório técnico ESALQ/Syngenta Piracicaba, p 1-13,
2005
TEIXEIRA, N.T.; ZAMBON, S.; BOLLELA, E.R,; NAKANO; OLIVEIRA, D.A; CALAFIORI,
M.H Adubação e aldicarb influenciando os teores de N, P e K, nas folhas da
cultura da batata (Solarium tuberosum L) Ecossistema, Espírito Santo do Pinhal,
v.16, p.120-125, 1991
VILLELA, F.A; DONI-FILHO,L,; SEQUEIRA,E.L Tabela de potencial osmótico em função
da concentração de polietileno glicol 6000 e da temperatura Pesquisa Agropecuária Brasileira, Brasília, v.26,n.11/12,p.1957-1968, 1991
Trang 8WHEATON, T A; CHILDERS, C.C.; TIMMER, L.W.; DUNCAN, L.W.; NIKDEL, S Effects of
aldicarb on the production, quality of fruits and situation of citrus plants in Florida Proceedings of the Florida State for Horticultural Society, Tallahasse, v 98, p 6-10,
1985
Trang 92
The Pyrethroid Knockdown Resistance
Ademir Jesus Martins and Denise Valle
Fundação Oswaldo Cruz/ Instituto Oswaldo Cruz/ Laboratório de Fisiologia e Controle de Artrópodes Vetores
Brazil
1 Introduction
New promising insect control efforts are now being evaluated such as biological alternatives
or even transgenic insects and Wolbachia based strategies Although it is increasingly clear
that successful approaches must involve integrated actions, chemical insecticides unfortunately still play a central role in pest and vector control (Raghavendra et al., 2011) Development of new safe and effective compounds in conjunction with preservation of those currently being utilized are important measures to insure insecticide availability and efficiency for arthropod control In this sense, understanding the interaction of insecticides with the insect organism (at physiological and molecular levels), the selected resistance mechanisms and their dynamics in and among natural populations is obligatory
Pyrethroids are synthetic compounds derived from pyrethrum, present in Chrysanthemum
flowers Currently, pyrethroids are the most used insecticides against arthropod plagues in agriculture and livestock as well as in the control of vectors of veterinary and human health importance They are chemically distinguished as type I (such as permethrin, compounds that lack an alpha-ciano group) and type II (with an alpha-ciano group, like deltamethrin) (T G Davies et al., 2007b) Pyrethroid insecticides have been largely adopted against vector mosquitoes through indoor, perifocal or ultra-low volume (ULV) applications As of yet pyrethroids are the only class of insecticides approved for insecticide treated nets (ITNs), an important tool under expansion against malaria, mainly in the African continent (Ranson et al., 2011) The consequence of intense and uncontrolled pyrethroid use is the extremely rapid selection of resistant populations throughout the world
Just like DDT, pyrethroids act very fast in the central nervous system of the insects, leading to
convulsions, paralysis and eventually death, an effect known as knockdown However, unlike
DDT, pyrethroids are not claimed to cause severe risks to the environment or to animal or human health, hence its widespread use The main pyrethroid resistance mechanism (the
knockdown resistance phenotype, kdr) occurs due to a point mutation in the voltage gated
sodium channel in the central nervous system, the target of pyrethroids and DDT
Herein we aim to discuss the main mechanism of pyrethroid resistance, the knockdown
resistance (kdr) mutation, its effect and its particularities among arthropods The most common methods presently employed to detect the kdr mutation are also discussed Some
aspects regarding the other main pyrethroid resistance mechanisms, like alterations in behaviour, cuticle and detoxifying enzymes will be only briefly addressed The proposal of this chapter is to review knockdown resistance to pyrethroids, nowadays the preferred insecticide class worldwide This topic discusses aspects of general biology, physiology,
Trang 10biochemistry, genetics and evolution, with focus on disease vector mosquitoes It is expected that the amount and diversity of material available on this subject may well illustrate insecticide resistance in a broader context
2 Insecticide resistance mechanisms
Besides the resistance to chemical insecticides caused by modifications in the target site (also called phenotypic resistance), other mechanisms commonly associated are: metabolic resistance, behavioral modification and alterations in the integument In the first case, endogenous detoxifying enzymes become more efficient in metabolizing the insecticide, preventing it from reaching its target in the nervous system This occurs due to 1) increase in the number of available molecules (by gene amplification or expression activation) or 2) mutation in the enzyme coding portion of the gene, so that its product metabolizes the insecticide more efficiently These processes can be very complex and involve three major enzyme superfamilies: Esterases, Multi function Oxidases P450 and Glutathion-S-Transferases (Hemingway & Ranson, 2000; Montella et al., 2007) In contrast, there are few examples in literature regarding insect behavioral changes and tegument alterations
Resistance to insecticides may be functionally defined as the ability of an insect population
to survive exposure to dosages of a given compound that are lethal to the majority of individuals of a susceptible lineage of the same species (Beaty & Marquardt, 1996) Resistance is based on the genetic variability of natural populations Under insecticide selection pressure, specific phenotypes are selected and consequently increase in frequency Resistance can result from the selection of one or more mechanisms In order to elucidate the molecular nature of resistance, many studies report laboratory controlled selection of different species (Chang et al., 2009; Kumar et al., 2002; Paeoporn et al., 2003; Rodriguez et al., 2003; Saavedra-Rodriguez et al., 2007) With selected lineages, it becomes easier to separate the role of each distinct mechanism In a more direct approach, the current availability of a series of molecular tools enables detection of expression of altered molecules
in model organisms so that the effect of the insecticide can be evaluated under specific and controlled circumstances (Smith et al., 1997)
Regardless of the mono or multi-factorial character of resistance, this phenomenon may be didactically divided into four categories: behavioral, cuticular, metabolic and phenotypic resistance In the first case the insect simply avoids contact with the insecticide through behavioral adaptations, which are presumably related to genetic inheritance (Sparks et al., 1989) Among arthropods, mosquitoes are by far the group most intensely investigated in
relation to behavioral resistance (Lockwood et al., 1984) For instance, Anopheles malaria
vector mosquitoes from the Amazon Region had the habit of resting in the walls after a blood meal There are registers that some populations changed their behavior after a period
of indoor residual application of DDT to the dwelling walls (Roberts & Alecrim, 1991) Behavioral changes that minimize contact between insect and insecticide may cause a severe impact in the insecticide application efficacy, especially if resistance is selected by physiological features (Ranson et al., 2011)
Certain alterations in the insect cuticle may reduce insecticide penetration However, these effects are unspecific, leading to resistance to a series of xenobiotic compounds This mechanism is known as reduced penetration or cuticle resistance It is probably not related
to high levels of resistance by itself, but it can interact synergistically with other mechanisms The physiological processes or molecular pathways which describe this type of